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xie, z.

Publications and source records attributed to xie, z..

2 recordsLinked to original sources

The CCCH Zinc Finger Gene PgCCCH50 from Pearl Millet Confers Drought and Salt Tolerance through an ABA-Dependent PgAREB1-PgCCCH50 Module

Abiotic stresses like drought and salinity severely constrain crop productivity. Pearl millet (Pennisetum glaucum L.), a stress-resilient cereal of global importance, is ideal for deciphering genetic adaptation. Although CCCH zinc finger proteins play key roles in plant stress responses, members with multiple regulatory functions remain unknown in this crop. This study analyzed 53 CCCH genes in pearl millet, examining their phylogeny, structure, chromosomal localization, and promoter cis-elements. Expression profiling revealed seven CCCH genes responsive to multiple stresses. Functional characterization of PgC3H50 showed that its overexpression in Arabidopsis conferred enhanced tolerance to drought and salt, evidenced by improved physiological parameters and upregulation of stress-responsive genes. We discovered that the ABA-responsive transcription factor PgAREB1(ABSCISIC ACID RESPONSIVE ELEMENT BINDING PROTEIN 1) directly binds to ABRE cis-elements in the PgC3H50 promoter and activates its transcription, validated by yeast one-hybrid, dual-luciferase, and EMSA assays. This defines a novel PgAREB1-PgC3H50 regulatory module within the ABA-mediated stress signaling pathway. Our findings provide a valuable genetic resource for the pearl millet CCCH family and unveil a promising candidate gene and transcriptional regulatory module for engineering crops with improved tolerance to drought and salinity. HighlightThis study reports the first genome-wide analysis of the CCCH family in pearl millet and identifies the novel PgAREB1-PgCCCH50 module as essential for salt and drought tolerance.

plant biology↗

PbrSYP71 regulates ER accumulation by interacting with actin during pollen tube growth in Pyrus

The uneven distribution of endoplasmic reticulum (ER) underlies the rapid polar growth of pollen tubes. However, the mechanism governing ER distribution remains elusive. In this study, we have identified a pollen tube-specific syntaxin protein, PbrSYP71. Our findings reveal that both overexpression and knocking down of PbrSYP71 inhibited pollen tube growth. Subcellular localization analysis demonstrates that PbrSYP71 anchors to the ER via its transmembrane structure. Overexpression of PbrSYP71 leads to clustered ER distribution in the pollen tube, while knocking down of PbrSYP71 abolishes the uneven ER distribution. Remarkably, transient overexpression of PbrSYP71{Delta}ABD, lacking the actin binding domain (ABD) of PbrSYP71, has no impact on ER distribution or pollen tube growth. Further investigation indicates that ABD is positioned on F-actin in the pollen tube and has a direct interaction with F-actin. PbrSYP71 assists the ER in moving towards the apex of pollen tube, with ABD displaying autonomous mobility. Our study elucidates that PbrSYP71 maintains uneven distribution of the ER by tethering ER to F-actin, facilitating ER movement towards the pollen tube apex for pear pollen tube elongation. These insights shed light on the mechanisms governing ER distribution in polarized cell growth.

cell biology↗